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Artículos de revistas sobre el tema "Proteaceae"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 25 de julio de 2025

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1

Hooper, Harvey. "Proteaceae." Ballarat Naturalist (1985:Sep) (September 1985): 7–8. http://dx.doi.org/10.5962/p.383841.

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2

Rourke, J. P. "PROTEACEAE." Bothalia 22, no. 1 (1992): 42. http://dx.doi.org/10.4102/abc.v22i1.821.

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3

Rourke, J. P. "PROTEACEAE." Bothalia 24, no. 2 (1994): 169–70. http://dx.doi.org/10.4102/abc.v24i2.767.

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4

Rourke, J. P. "PROTEACEAE." Bothalia 26, no. 2 (1996): 154–57. http://dx.doi.org/10.4102/abc.v26i2.700.

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5

Rourke, J. P. "PROTEACEAE." Bothalia 27, no. 1 (1997): 52–55. http://dx.doi.org/10.4102/abc.v27i1.658.

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6

Rouke, J. P. "PROTEACEAE." Bothalia 35, no. 1 (2005): 63–67. http://dx.doi.org/10.4102/abc.v35i1.370.

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7

Stace, Helen M., Andrew W. Douglas, and Jane F. Sampson. "Did ‘Paleo-polyploidy’ Really occur in Proteaceae?" Australian Systematic Botany 11, no. 4 (1998): 613. http://dx.doi.org/10.1071/sb98013.

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Cytological data for 188 species in 65 genera of Proteaceae were collated from the literature. Excluding the occasional infrageneric polyploid, Proteaceae have seven confirmed character states for chromosome number (n = 14, 13, 12, 11, 10, 7, 5). Genera of subfamily Persoonioideae are x = 7, and, on a cytoevolutionary doctrine of ‘paleo-polyploidy’ in angiosperm families, these low chromosome number taxa were hypothesised to represent the ancestral genome of Proteaceae. Chief supporting evidence for this hypothesis is the ancient origin of Persoonioideae in Proteaceae phylogeny. However all cu

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8

Hayes, Patrick E., Peta L. Clode, Caio Guilherme Pereira, and Hans Lambers. "Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia." Journal of Experimental Botany 70, no. 15 (2019): 3995–4009. http://dx.doi.org/10.1093/jxb/erz156.

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Abstract Over 650 Proteaceae occur in south-western Australia, contributing to the region’s exceptionally high biodiversity. Most Proteaceae occur exclusively on severely nutrient-impoverished, acidic soils (calcifuge), whilst only few also occur on young, calcareous soils (soil-indifferent), higher in calcium (Ca) and phosphorus (P). The calcifuge habit of Proteaceae is explained by Ca-enhanced P toxicity, putatively linked to the leaf cell-specific allocation of Ca and P. Separation of these elements is essential to avoid the deleterious precipitation of Ca-phosphate. We used quantitative X-

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9

Malan, Daniel G. "PROPAGATION OF PROTEACEAE." Acta Horticulturae, no. 316 (December 1992): 27–34. http://dx.doi.org/10.17660/actahortic.1992.316.5.

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10

Prance, Ghillean T., and Vanessa Plana. "The American Proteaceae." Australian Systematic Botany 11, no. 4 (1998): 287. http://dx.doi.org/10.1071/sb97023.

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The American Proteaceae are outliers from the main centres of diversity of the family in Australia and South Africa. There are about 83 species in eight genera which all belong to the monophyletic subfamily Grevilleoideae. Three genera, Embothrium, Oreocallis and Lomatia, are placed in the tribe Embothrieae (sensu Johnson and Briggs), four Euplassa, Gevuina, Panopsis and Roupala in the Macadamieae and the single genus Orites in the Oriteae. There are five genera endemic to America and three also have species in Australia and New Guinea (Gevuina, Lomatia and Orites). The Proteaceae appear to ha

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11

Pole, Mike. "The Proteaceae record in New Zealand." Australian Systematic Botany 11, no. 4 (1998): 343. http://dx.doi.org/10.1071/sb97019.

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Proteaceae pollen appeared in New Zealand during the Late Cretaceous and increased in diversity until the Early–mid Eocene. Diversity then decreased, reducing to the present two species in the Early Pleistocene. Proteaceae macrofossils extend back to the Early Paleocene. Twelve parataxa of Proteaceae dispersed cuticle are documented. These include two new parataxa of unknown affinity from the Paleocene, and nine new parataxa from the Miocene and one previously recorded from Western Australia. Three of these are identified as species of Helicia, Macadamia and Musgravea, one has affinities with

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12

Zhang, Jiale, Michael E. Netzel, Andrew Pengelly, Dharini Sivakumar, and Yasmina Sultanbawa. "A Review of Phytochemicals and Bioactive Properties in the Proteaceae Family: A Promising Source of Functional Food." Antioxidants 12, no. 11 (2023): 1952. http://dx.doi.org/10.3390/antiox12111952.

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In recent decades, natural plant-based foods have been increasingly used to improve human health due to unhealthy modern dietary patterns, such as the consumption of foods high in sugar and fat. Many indigenous species have been used by Aboriginal peoples for their food and therapeutic properties. Thus, it is important to understand the health-enhancing bioactive profile of Australian indigenous species. The Proteaceae family, such as the genera of Protea, Macadamia, and Grevillea, have been commercially used in the horticulture and food industries. Researchers have reported some findings abou

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13

PYE, DANIEL R. L. "A new species of eriophyoid mite (Acari: Eriophyoidea: Eriophyidae) on Leucadendron argenteum (L.) R. Br. from South Africa." Zootaxa 3085, no. 1 (2011): 63. http://dx.doi.org/10.11646/zootaxa.3085.1.5.

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A new vagrant eriophyoid mite species, collected from plant material imported into the United Kingdom, is described and illustrated: Aceria argentae n. sp. found on Leucadendron argenteum (L.) R. Br. (Proteaceae) from South Africa. A review of the eriophyoid mite species known from plants in the Proteaceae is also provided and recent findings of non-native eriophyoid mites in the United Kingdom are discussed.

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14

MAZZEO, GAETANA, JOSÉ CARLOS FRANCO, and AGATINO RUSSO. "A new Paracoccus species from Palaearctic region (Hemiptera, Sternorrhyncha, Coccoidea, Pseudococcidae)." Zootaxa 2274, no. 1 (2009): 62–68. http://dx.doi.org/10.11646/zootaxa.2274.1.4.

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A new mealybug species, Paracoccus leucadendri sp. nov., is described from Portugal. This is the first record of a Paracoccus species from Europe. It is suggested that its presence in Portugal is the result of a fortuitous introduction with its host plant, Leucadendron sp. (Proteaceae). An identification key is presented to distinguish this new Paracoccus species from other mealybug species reported on Proteaceae in the world.

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15

Itzstein-Davey, Freea. "The representation of Proteaceae in modern pollen rain in species-rich vegetation communities in south-western Australia." Australian Journal of Botany 51, no. 2 (2003): 135. http://dx.doi.org/10.1071/bt02048.

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The Proteaceae family is a large Gondwanan plant family with a major centre of richness in south-western Australia. Modern pollen–vegetation relationships in the two areas of species richness in the northern and southern sandplains of south-western Australia were investigated to calibrate fossil-pollen studies concurrently conducted on Eocene, Pliocene and Quaternary sediment. Results indicated that the Proteaceae component in modern pollen rain can be quite high, contributing up to 50% of the count. Some sites showed a dominant type (such as Banksia–Dryandra), whilst others had up to six diff

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16

Crous, P. W., B. A. Summerell, L. Swart, et al. "Fungal pathogens of Proteaceae." Persoonia - Molecular Phylogeny and Evolution of Fungi 27, no. 1 (2011): 20–45. http://dx.doi.org/10.3767/003158511x606239.

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17

Johnson, L. A. S. "Proteaceae - Where are we?" Australian Systematic Botany 11, no. 4 (1998): 251. http://dx.doi.org/10.1071/sb97024.

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Developments in understanding of the Proteaceae since 1963 are briefly reviewed and discussed in relation to morphological interpretation, DNA studies, phytogeography and phylogeny. Some of the outstanding questions are highlighted. Starting Point More than 30 years ago, Barbara Briggs and I (Johnson and Briggs 1963) published a hypothesis of the phylogeny of Proteaceae, a family of great interest for which no reasonably acceptable evolutionary history had been proposed. Unfortunately, at the time we wrote this paper, we were misled by conservative geologists who had not got around to acceptin

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18

Swenson, Wendy K., John E. Dunn, and Eric E. Conn. "Cyanogenesis in the proteaceae." Phytochemistry 28, no. 3 (1989): 821–23. http://dx.doi.org/10.1016/0031-9422(89)80122-0.

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19

Pearce, Ceridwen A., Paul Reddell, and Kevin D. Hyde. "Revision of the Phyllachoraceae (Ascomycota) on hosts in the angiosperm family, Proteaceae." Australian Systematic Botany 14, no. 2 (2001): 283. http://dx.doi.org/10.1071/sb00006.

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A literature review yielded seven Australian taxa within the Phyllachoraceae recorded from hosts in the angiosperm family Proteaceae, with three taxa from overseas. New collections and herbarium material were examined by using traditional microscopic characters. Seven new Australian taxa were identified. These include Phyllachora banksiae subsp. westaustraliensis on Banksia speciosa, Phyllachora tjapukiensis on Darlingia darlingiana, Phyllachora kylei on Dryandra spp., Phyllachora amplexicaulii on Hakea amplexicaulis, Phyllachora grevilleae subsp. clelandii on Hakea clavata and H. vittata, Phy

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20

Lamont, Byron B., and Philip G. Ladd. "Endobeuthos paleosum in 99-million-year-old amber does not belong to the Proteaceae." Journal of the Botanical Research Institute of Texas 18, no. 1 (2024): 143–47. http://dx.doi.org/10.17348/jbrit.v18.i1.1343.

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Species in the family Proteaceae are almost invariably tetramerous with the stamen adnate to a tepal. Andromonoecious inflorescences bearing many male flowers composed of a single (spathuloid) stamen and a female flower with a pubescent stigma, as in Endobeuthos paleosum, are unknown. We suggest that the specimen is a bisexual flower with scores of stamens surrounding a single stigma-style. Further, the specimen is too old to fit with current understanding of the migratory history of the Proteaceae.

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21

Pujana, Roberto R. "New fossil woods of Proteaceae from the Oligocene of southern Patagonia." Australian Systematic Botany 20, no. 2 (2007): 119. http://dx.doi.org/10.1071/sb06029.

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The scarce fossil wood record of Proteaceae is complemented with the addition of a new morphogenus with two new species from the Oligocene of Patagonia, Scalarixylon patagonicum, gen. nov., sp. nov., and S. grandiradiatum, gen. nov., sp. nov. They become the first two fossil species that have all the typical characteristics of Proteaceae wood anatomy: wide multiseriate rays, tangential bands of vessels with unilateral banded associated parenchyma and simple perforation plates. They seem to be related to extant species that inhabit the subantarctic forests of Patagonia.

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22

Skelton, R. P., J. J. Midgley, J. M. Nyaga, S. D. Johnson, and M. D. Cramer. "Is leaf pubescence of Cape Proteaceae a xeromorphic or radiation-protective trait?" Australian Journal of Botany 60, no. 2 (2012): 104. http://dx.doi.org/10.1071/bt11231.

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Although pubescence has traditionally been considered to be related to the water economy of plants, the results are ambivalent and vary between different species. We tested two contrasting hypotheses for the functional significance of leaf pubescence of Proteaceae species from the Cape Floristic Region. First, we hypothesised that pubescence is a xeromorphic trait that conserves water by increasing the boundary layer resistance to diffusion. Water loss was measured in two morphotypes of Leucospermum conocarpodendron (L.) Buek that differ in the degree of leaf pubescence, using both gas exchang

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23

Cowling, Richard M., and Byron B. Lamont. "On the Nature of Gondwanan Species Flocks: Diversity of Proteaceae in Mediterranean South-western Australia and South Africa." Australian Journal of Botany 46, no. 4 (1998): 335. http://dx.doi.org/10.1071/bt97040.

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The Proteaceae, a Gondwanan family, are richly represented in South Africa’s Cape Floristic Region (CFR) (331 species, 14 genera) and Australia’s South West Botanical Province (SWBP) (682 species, 16 genera). Both of these regions have mediterranean-type climates, infertile soils, similar geomorphic and climatic histories, and show strong convergences in plant form and function. There are many similarities in the patterns and ecological correlates of diversity in the CFR and SWBP Proteaceae. First, both floras are overwhelmingly endemic, with many large genera and correspondingly high species

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24

Lee, Seonju, J. Z. (Ewald) Groenewald, Joanne E. Taylor, Francois Roets, and Pedro W. Crous. "Rhynchostomatoid Fungi Occurring on Proteaceae." Mycologia 95, no. 5 (2003): 902. http://dx.doi.org/10.2307/3762018.

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25

Montarone, M., and P. Allemand. "GROWING PROTEACEAE SOILLESS UNDER SHELTER." Acta Horticulturae, no. 387 (June 1995): 73–84. http://dx.doi.org/10.17660/actahortic.1995.387.8.

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26

Midgley, J. J., and J. Vlok. "FLOWERING PATTERNS IN CAPE PROTEACEAE." Acta Horticulturae, no. 185 (June 1986): 273–76. http://dx.doi.org/10.17660/actahortic.1986.185.32.

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27

Weston, Peter. "A revision of Hicksbeachia (Proteaceae)." Telopea 3, no. 2 (1988): 231–39. http://dx.doi.org/10.7751/telopea19884810.

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28

Barker, Robyn, and Bill Barker. "Plate 464. Hakea Rhombales Proteaceae." Curtis's Botanical Magazine 20, no. 2 (2003): 69–73. http://dx.doi.org/10.1111/1467-8748.00374.

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29

Hooper, Harvey. "Proteaceae – continued from Sept 1985." Ballarat Naturalist (1985:Oct) (October 1985): 8. http://dx.doi.org/10.5962/p.383845.

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30

Feuer, Sylvia. "Pollen Morphology of Embothrieae (Proteaceae)." Grana 28, no. 4 (1989): 225–42. http://dx.doi.org/10.1080/00173138909427438.

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31

Swart, L., P. W. Crous, S. Denman, and M. E. Palm. "Fungi occurring on Proteaceae. I." South African Journal of Botany 64, no. 2 (1998): 137–45. http://dx.doi.org/10.1016/s0254-6299(15)30848-6.

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32

Lee, Seonju, J. Z. (Ewald) Groenewald, Joanne E. Taylor, Francois Roets, and Pedro W. Crous. "Rhynchostomatoid fungi occurring on Proteaceae." Mycologia 95, no. 5 (2003): 902–10. http://dx.doi.org/10.1080/15572536.2004.11833049.

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33

Criley, Richard A. "PROTEACEAE: BEYOND THE BIG THREE." Acta Horticulturae, no. 545 (February 2001): 79–85. http://dx.doi.org/10.17660/actahortic.2001.545.11.

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34

Robyn, Adele, Gail M. Littlejohn, and Henry Allies. "SEEDBANKS OF SOUTHERN AFRICAN PROTEACEAE." Acta Horticulturae, no. 545 (February 2001): 29–33. http://dx.doi.org/10.17660/actahortic.2001.545.2.

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35

Pérez-Francés, J. F., V. Raya Ramallo, and J. A. Rodríguez-Pérez. "MICROPROPAGATION OF LEUCOSPERMUM `SUNRISE´ (PROTEACEAE)." Acta Horticulturae, no. 545 (February 2001): 161–69. http://dx.doi.org/10.17660/actahortic.2001.545.22.

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36

Verotta, L., F. Orsini, F. Pelizzoni, G. Torri, and C. B. Rogers. "Polyphenolic Glycosides from African Proteaceae." Journal of Natural Products 62, no. 11 (1999): 1526–31. http://dx.doi.org/10.1021/np9902237.

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37

Carpenter, Raymond J., Jennifer M. Bannister, Daphne E. Lee, and Gregory J. Jordan. "Proteaceae leaf fossils from the Oligo - Miocene of New Zealand: new species and evidence of biome and trait conservatism." Australian Systematic Botany 25, no. 6 (2012): 375. http://dx.doi.org/10.1071/sb12018.

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At least seven foliar taxa of Proteaceae occur in Oligo–Miocene lignite from the Newvale site. These taxa include two new species of the fossil genus Euproteaciphyllum, and previously described species of tribe Persoonieae and Banksia. Other specimens from Newvale are not assigned to new species, but some conform to leaves of the New Caledonian genus Beauprea, which is also represented in the lignite by common pollen. Two other Euproteaciphyllum species are described from the early Miocene Foulden Maar diatomite site. One of these species may belong to Alloxylon (tribe Embothrieae) and the oth

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38

Chambers, Kenton L., and George O. Poinar, Jr. "Reinterpretation of the mid-Cretaceous fossil flower Endobeuthos paleosum as a capitular, unisexual inflorescence of Proteaceae." Journal of the Botanical Research Institute of Texas 17, no. 2 (2023): 449–56. http://dx.doi.org/10.17348/jbrit.v17.i2.1324.

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The Myanmar amber fossil Endobeuthos paleosum was originally described as composed of an individual flower with a calyx of numerous, helically arranged sepals, a whorl of petals, and 60+ stamens each bearing a single bisporangiate anther. The 6 flowers, embedded together in a single block of amber, were described as varying in their calyx pubescence and length of corolla segments. The numerous stamens, with their single anther, led to a hypothesized relationship with certain members of family Dilleniaceae. We now propose a complete reinterpretation of this fossil as being an involucrate capitu

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39

Grinbergs, Janis, Eduardo Valenzuela, and Carlos Ramirez. "GERMINACION "IN VITRO" DE GEVUINA AVELLANA MOL. (PROTEACEAE)." Bosque 7, no. 2 (1986): 95–101. http://dx.doi.org/10.4206/bosque.1986.v7n2-05.

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40

Carpenter, RJ, and M. Pole. "Eocene plant fossils from the Lefroy and Cowan paleodrainages, Western Australia." Australian Systematic Botany 8, no. 6 (1995): 1107. http://dx.doi.org/10.1071/sb9951107.

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Forty-two dispersed cuticle taxa are described from late Middle Eocene drill core samples in the Lefroy and Cowan paleodrainages (Kambalda–Norseman region), Western Australia. They are preserved in fluvial-marginal marine sediments of the Pidinga and Werillup Formations. Thirty-four distinct cuticle taxa occur in the richest sample including Cupressaceae, Araucariaceae (Agathis), Podocarpaceae (Dacrycarpus, Acmopyle, Dacrydium), Cunoniaceae, Lauraceae, Myrtaceae, Casuarinaceae (Gymnostoma), Nothofagus subgenus Lophozonia and tribes Embothrieae, Macadamieae and Banksieae of the Proteaceae. The

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41

Bellgard, SE. "Mycorrhizal Associations of Plant-Species in Hawkesbury Sandstone Vegetation." Australian Journal of Botany 39, no. 4 (1991): 357. http://dx.doi.org/10.1071/bt9910357.

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The mycorrhizal associations of plant species in an open woodland and heathland on Hawkesbury Sandstone soils were examined. The two geographically disjunct sites supported vegetation of differing physiognomy, but possessed many species common to both sites. At the woodland site, 21 of the 32 plant species examined had mycorrhizal associations. At the heath site, 31 of the 47 plant species examined were mycorrhizal. Mycorrhizal associations were found on representatives of the Cyperaceae and Proteaceae, families not previously thought to be mycorrhizal. Internal hyphae, vesicles, and cortical

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42

Jordan, Gregory J., Raymond J. Carpenter, Barbara R. Holland, Nicholas J. Beeton, Michael D. Woodhams, and Timothy J. Brodribb. "Links between environment and stomatal size through evolutionary time in Proteaceae." Proceedings of the Royal Society B: Biological Sciences 287, no. 1919 (2020): 20192876. http://dx.doi.org/10.1098/rspb.2019.2876.

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The size of plant stomata (adjustable pores that determine the uptake of CO 2 and loss of water from leaves) is considered to be evolutionarily important. This study uses fossils from the major Southern Hemisphere family Proteaceae to test whether stomatal cell size responded to Cenozoic climate change. We measured the length and abundance of guard cells (the cells forming stomata), the area of epidermal pavement cells, stomatal index and maximum stomatal conductance from a comprehensive sample of fossil cuticles of Proteaceae, and extracted published estimates of past temperature and atmosphe

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43

Clode, Peta L. "A Method for Preparing Difficult Plant Tissues for Light and Electron Microscopy." Microscopy and Microanalysis 21, no. 4 (2015): 902–9. http://dx.doi.org/10.1017/s1431927615013756.

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AbstractAlthough the advent of microwave technologies has both improved and accelerated tissue processing for microscopy, there still remain many limitations in conventional chemical fixation, dehydration, embedding, and sectioning, particularly with regard to plant materials. The Proteaceae, a family of plants widely distributed in the Southern Hemisphere and well adapted to harsh climates and nutrient-poor soils, is a perfect example; the complexity of Proteaceae leaves means that almost no ultrastructural data are available as these are notoriously difficult to both infiltrate and section.

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44

Hawkins, Heidi-J., Hans Hettasch, Adam G. West, and Michael D. Cramer. "Hydraulic redistribution by Protea 'Sylvia' (Proteaceae) facilitates soil water replenishment and water acquisition by an understorey grass and shrub." Functional Plant Biology 36, no. 8 (2009): 752. http://dx.doi.org/10.1071/fp09046.

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Proteaceae of the Cape Floristic Region, South Africa, transpire throughout the summer drought, implying access to deep water. Hydraulic redistribution by Protea ‘Sylvia’ [P. susannae E. Phillips × P. exima (Salisb. Ex Knight) Fource; Proteaceae] was investigated in overnight pot and field experiments, where it was hypothesised that (1) Proteaceae replenish water in upper soil layers, (2) hydraulic redistribution facilitates nutrient uptake and (3) shallow-rooted understorey plants ‘parasitise’ water from proteas. Potted Sylvias redistributed ~17% of the tritiated water supplied, equating to 3

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45

Hoot, Sara B., and Andrew W. Douglas. "Phylogeny of the Proteaceae based on atpB and atpB-rbcL intergenic spacer region sequences." Australian Systematic Botany 11, no. 4 (1998): 301. http://dx.doi.org/10.1071/sb98027.

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Parsimony analyses were conducted for 46 genera representing all subfamilies and tribes within Proteaceae using two chloroplast sequences: the gene atpB and the noncoding spacer region between atpB and rbcL. The spacer region was more variable than atpB and provided insertion and deletion data as well as nucleotide substitutions. The atpB and spacer region data sets were highly congruent (as indicated by the partition homogeneity test) and were analysed separately and combined. Both unweighted and weighted character states (3 : 1 correction for transition bias) for the atpB data resulted in ve

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46

Taylor, Gary S., and Melinda L. Moir. "Further evidence of the coextinction threat for jumping plant-lice: three new Acizzia (Psyllidae) and Trioza (Triozidae) from Western Australia." Insect Systematics & Evolution 45, no. 3 (2014): 283–302. http://dx.doi.org/10.1163/1876312x-00002107.

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Three new species of jumping plant-lice (Psylloidea) are described from Western Australia. Acizzia hughesae sp.n. occurs on Acacia veronica Maslin (Fabaceae: Mimosoideae), A. mccarthyi sp.n. on an undescribed species of Grevillea (Proteaceae) identified by the Western Australian State Government as in need of conservation action (Grevillea sp. ‘Stirling Range’) and Trioza barrettae sp.n. from the critically endangered Banksia brownii (Proteaceae). These new species of jumping plant-lice are considered rare, and at risk of extinction, or coextinction, as they are recorded from plant species wit

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47

Carpenter, Raymond J., Gregory J. Jordan, and Robert S. Hill. "Fossil leaves of Banksia, Banksieae and pretenders: resolving the fossil genus Banksieaephyllum." Australian Systematic Botany 29, no. 2 (2016): 126. http://dx.doi.org/10.1071/sb16005.

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The genus Banksieaephyllum, originally erected for cuticle-bearing fossil leaves of subtribe Banksiinae (Proteaceae subfamily Grevilleoideae, tribe Banksieae), is reassessed. Of the 18 described species, nine are accepted within Banksia, including Banksieaephyllum obovatum Cookson & Duigan, which is synonymised with B. laeve Cookson & Duigan on the basis of new cuticular preparations. Two other species are transferred to Banksieaefolia gen. nov., a genus erected for Banksieae of uncertain affinities, and which presently includes only fossils that probably belong to subtribe Musgraveina

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Edwards, K. S., and G. T. Prance. "Four new species of Roupala (Proteaceae)." Brittonia 55, no. 1 (2003): 61–68. http://dx.doi.org/10.1663/0007-196x(2003)055[0061:fnsorp]2.0.co;2.

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Jordan, Gregory J., Timothy J. Brodribb, Christopher J. Blackman, and Peter H. Weston. "Climate drives vein anatomy in Proteaceae." American Journal of Botany 100, no. 8 (2013): 1483–93. http://dx.doi.org/10.3732/ajb.1200471.

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Marincowitz, S., J. Z. Groenewald, M. J. Wingfield, and P. W. Crous. "Species of Botryosphaeriaceae occurring on Proteaceae." Persoonia - Molecular Phylogeny and Evolution of Fungi 21, no. 1 (2008): 111–18. http://dx.doi.org/10.3767/003158508x372387.

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